Manufacturing Associate I
Moderna
October 1, 2026
Full-time
On-site
Norwood, MA
Operations
Role: Manufacturing Associate I in mRNA and LNP drug substance operations, executing GMP manufacturing processes for clinical and commercial vaccine products. Responsibilities: perform aseptic processing, formulation, filling, and dispensing of drug substances in a clean-room environment; ensure GMP compliance, proper documentation, data integrity, and environmental safety; operate support systems like SAP, VEEVA, Delta V, and LIMS; troubleshoot basic equipment issues; adhere to safety and waste handling procedures. Requirements: HS Diploma with 3-5 years' industry experience or STEM/Associates' degree with 2-3 years' experience; ability to learn GMP regulations; prior sterile manufacturing experience preferred. High-Value: GMP manufacturing, aseptic drug processing, mRNA/LNP technology, clinical and commercial vaccine production, on-site work, no travel requirement. WorkSetup: 100% onsite in a GMP environment.